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   Genetics of long-QT syndrome  
   
نویسنده Nakano Yukiko ,Shimizu Wataru
منبع journal of human genetics - 2016 - دوره : 61 - شماره : 1 - صفحه:51 -55
چکیده    Congenital long qt syndrome (lqts) is an inherited arrhythmia syndrome characterized by a prolonged qt interval in the 12-lead ecg, torsades de pointes and not negligible prevalence of sudden cardiac death. the genetic testing plays an important role in the diagnosis of lqts. a total of 15 genes have been reported for autosomal-dominant forms of romano–ward-type congenital lqts and 2 genes for autosomal-recessive forms of the jervell and lange–nielsen syndrome. in this review, we summarize the recent advances in genetics of lqts and briefly describe forward perspectives of lqts investigation.
آدرس Hiroshima University, Division of Frontier Medical Science, Department of Cardiovascular Medicine, Japan, Nippon Medical School, Department of Cardiovascular Medicine, Japan
 
     
   
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